Ali Bin Ali Holding
Premier réseau de distribution du Qatar pour les importations de produits de consommation et d'équipements médicaux
Ali Bin Ali Holding gère des structures d'approvisionnement complètes pour les actifs pharmaceutiques et les produits de luxe des marques mondiales d'épicerie. Leurs centres de distribution offrent une couverture à grande échelle pour les réseaux de vente au détail et de soins de santé des entreprises.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Doha, Qatar
- Founded
- 1945
- Website
- alibinali.com
- Categories
- Épicerie sèche, Hygiène et soins personnels, Fournitures médicales et de santé
- Markets
- Qatar, Arabie saoudite
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 22000, Food Safety IAF CertSearch
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)